CA2573802C - High gloss, non-feathering lip product comprising a water-insoluble polysaccharide and a polyol ester - Google Patents
High gloss, non-feathering lip product comprising a water-insoluble polysaccharide and a polyol ester Download PDFInfo
- Publication number
- CA2573802C CA2573802C CA2573802A CA2573802A CA2573802C CA 2573802 C CA2573802 C CA 2573802C CA 2573802 A CA2573802 A CA 2573802A CA 2573802 A CA2573802 A CA 2573802A CA 2573802 C CA2573802 C CA 2573802C
- Authority
- CA
- Canada
- Prior art keywords
- shine
- composition
- feathering
- polyol ester
- product
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- -1 polyol ester Chemical class 0.000 title claims abstract description 29
- 229920005862 polyol Polymers 0.000 title claims abstract description 23
- 229920001282 polysaccharide Polymers 0.000 title abstract description 17
- 150000004676 glycans Chemical class 0.000 title abstract description 15
- 239000005017 polysaccharide Substances 0.000 title abstract description 15
- 239000000203 mixture Substances 0.000 claims abstract description 49
- 239000007788 liquid Substances 0.000 claims abstract description 18
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical group CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims abstract description 13
- 235000019325 ethyl cellulose Nutrition 0.000 claims abstract description 11
- 229920001249 ethyl cellulose Polymers 0.000 claims abstract description 11
- 239000001856 Ethyl cellulose Substances 0.000 claims abstract description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims abstract description 5
- GHVNFZFCNZKVNT-UHFFFAOYSA-M decanoate Chemical compound CCCCCCCCCC([O-])=O GHVNFZFCNZKVNT-UHFFFAOYSA-M 0.000 claims abstract description 4
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 claims abstract description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims abstract description 4
- 230000000699 topical effect Effects 0.000 claims abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 44
- 150000002191 fatty alcohols Chemical class 0.000 claims description 21
- 239000000377 silicon dioxide Substances 0.000 claims description 21
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 14
- 239000000194 fatty acid Substances 0.000 claims description 14
- 229930195729 fatty acid Natural products 0.000 claims description 14
- 239000000049 pigment Substances 0.000 claims description 11
- 235000000346 sugar Nutrition 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 229910021485 fumed silica Inorganic materials 0.000 claims description 2
- 239000002537 cosmetic Substances 0.000 abstract description 9
- 239000000047 product Substances 0.000 description 34
- 239000003921 oil Substances 0.000 description 14
- 235000019198 oils Nutrition 0.000 description 14
- 150000002148 esters Chemical class 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 11
- 150000003077 polyols Chemical class 0.000 description 10
- 239000002245 particle Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000003974 emollient agent Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 4
- 229920002678 cellulose Polymers 0.000 description 4
- 235000010980 cellulose Nutrition 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 229940008099 dimethicone Drugs 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 150000002194 fatty esters Chemical class 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 230000002045 lasting effect Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 2
- GLCFQKXOQDQJFZ-UHFFFAOYSA-N 2-ethylhexyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(CC)CCCC GLCFQKXOQDQJFZ-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 2
- 229940073609 bismuth oxychloride Drugs 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000013270 controlled release Methods 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 235000013980 iron oxide Nutrition 0.000 description 2
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 150000002772 monosaccharides Chemical group 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229920001542 oligosaccharide Polymers 0.000 description 2
- 150000002482 oligosaccharides Chemical class 0.000 description 2
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 1
- GYDYJUYZBRGMCC-INIZCTEOSA-N (2s)-2-amino-6-(dodecanoylamino)hexanoic acid Chemical compound CCCCCCCCCCCC(=O)NCCCC[C@H](N)C(O)=O GYDYJUYZBRGMCC-INIZCTEOSA-N 0.000 description 1
- NRTKYSGFUISGRQ-UHFFFAOYSA-N (3-heptanoyloxy-2,2-dimethylpropyl) heptanoate Chemical compound CCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCC NRTKYSGFUISGRQ-UHFFFAOYSA-N 0.000 description 1
- UMPNFVHHMOSNAC-WLDMJGECSA-N (3r,4s,5s,6r)-6-(hydroxymethyl)-3-methoxyoxane-2,4,5-triol Chemical compound CO[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O UMPNFVHHMOSNAC-WLDMJGECSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- IAFBRPFISOTXSO-UHFFFAOYSA-N 2-[[2-chloro-4-[3-chloro-4-[[1-(2,4-dimethylanilino)-1,3-dioxobutan-2-yl]diazenyl]phenyl]phenyl]diazenyl]-n-(2,4-dimethylphenyl)-3-oxobutanamide Chemical compound C=1C=C(C)C=C(C)C=1NC(=O)C(C(=O)C)N=NC(C(=C1)Cl)=CC=C1C(C=C1Cl)=CC=C1N=NC(C(C)=O)C(=O)NC1=CC=C(C)C=C1C IAFBRPFISOTXSO-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
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- 229910052782 aluminium Inorganic materials 0.000 description 1
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- 125000004429 atom Chemical group 0.000 description 1
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- UHHXUPJJDHEMGX-UHFFFAOYSA-K azanium;manganese(3+);phosphonato phosphate Chemical compound [NH4+].[Mn+3].[O-]P([O-])(=O)OP([O-])([O-])=O UHHXUPJJDHEMGX-UHFFFAOYSA-K 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
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- 235000019425 dextrin Nutrition 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 description 1
- YGANSGVIUGARFR-UHFFFAOYSA-N dipotassium dioxosilane oxo(oxoalumanyloxy)alumane oxygen(2-) Chemical compound [O--].[K+].[K+].O=[Si]=O.O=[Al]O[Al]=O YGANSGVIUGARFR-UHFFFAOYSA-N 0.000 description 1
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- HJXPPCPJEYUQFQ-HNNXBMFYSA-N dodecyl (2s)-5-oxopyrrolidine-2-carboxylate Chemical compound CCCCCCCCCCCCOC(=O)[C@@H]1CCC(=O)N1 HJXPPCPJEYUQFQ-HNNXBMFYSA-N 0.000 description 1
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- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
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- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
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- FOYKKGHVWRFIBD-UHFFFAOYSA-N gamma-tocopherol acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 FOYKKGHVWRFIBD-UHFFFAOYSA-N 0.000 description 1
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- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 239000001056 green pigment Substances 0.000 description 1
- HNMCSUXJLGGQFO-UHFFFAOYSA-N hexaaluminum;hexasodium;tetrathietane;hexasilicate Chemical class [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].S1SSS1.S1SSS1.[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] HNMCSUXJLGGQFO-UHFFFAOYSA-N 0.000 description 1
- ZBMAXVLMNGIJSD-KZTXLXSCSA-N hexadecanoic acid (3R,4S,5R,6R)-3,4,5,6,7-pentahydroxyheptan-2-one Chemical compound CC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCCCCCCCCCC(O)=O ZBMAXVLMNGIJSD-KZTXLXSCSA-N 0.000 description 1
- HKPGZZNQPUBKGQ-KAVXHDQVSA-N hexadecanoic acid (4R,5S,6R,7R)-4,5,6,7,8-pentahydroxyoctan-3-one Chemical compound CCC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCCCCCCCCCC(O)=O HKPGZZNQPUBKGQ-KAVXHDQVSA-N 0.000 description 1
- UCZNZRYBJXGIAV-SSPAHAAFSA-N hexadecanoic acid;(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanal Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O.CCCCCCCCCCCCCCCC(O)=O UCZNZRYBJXGIAV-SSPAHAAFSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000832 lactitol Substances 0.000 description 1
- 235000010448 lactitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-JVCRWLNRSA-N lactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-JVCRWLNRSA-N 0.000 description 1
- 229960003451 lactitol Drugs 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
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- 229940035436 maltitol Drugs 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
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- 230000001333 moisturizer Effects 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 229910052627 muscovite Inorganic materials 0.000 description 1
- PYUYQYBDJFMFTH-WMMMYUQOSA-N naphthol red Chemical compound CCOC1=CC=CC=C1NC(=O)C(C1=O)=CC2=CC=CC=C2\C1=N\NC1=CC=C(C(N)=O)C=C1 PYUYQYBDJFMFTH-WMMMYUQOSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000001053 orange pigment Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940032085 sucrose monolaurate Drugs 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- HJUSCZXBOMVODD-UHFFFAOYSA-N tetradecyl octanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCC HJUSCZXBOMVODD-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Abstract
The invention addresses the need for high gloss, non-feathering topical compositions, especially lip products. Current high shine lipsticks typically have little staying power on the lips and give rise to moderate to severe feathering. Attempts to remedy this problem have not been completely satisfactory, as regards the amount of shine, amount of staying power, the overall look or feel of the composition. The present invention meets the need for a high shine cosmetic composition that avoids unattractive feathering and short wear problems, by providing a composition comprising at least one water-insoluble, fatty alcohol-soluble polysaccharide and a liquid polyol ester.
Preferably, the polysaccharide is ethylcellulose, and the liquid polyol ester is pentaerythrityl adipate/caprate/caprylate/heptanoate.
Preferably, the polysaccharide is ethylcellulose, and the liquid polyol ester is pentaerythrityl adipate/caprate/caprylate/heptanoate.
Description
HIGH GLOSS, NON-FEATHERING LIP PRODUCT COMPRISING A WATER-INSOLUBLE POLYSACCHARIDE AND A POLYOL ESTER
Field of the Invention The invention relates to cosmetic compositions. In particular, the invention relates to color cosmetics, particularly lip products.
Background of the Invention Lip products come in a variety of forms, which vary depending upon the look desired by the user. The products may be highly pigmented, pearlescent, matte, or glossy/shiny. The latter type, i.e., the high gloss type of lip color, is currently particularly popular, especially among young women.
The look conferred by such a product is highly glamorous and sensual, but has several drawbacks associated with it. The current technology available to produce a high shine lipstick is such that those lipstick or glosses giving the best shine typically have little staying power on the lips. In addition, these products also give rise to moderate to severe feathering, a condition in which the pigment intended to color the lips actually migrates into the fine lines around the mouth, producing a smeared, unattractive appearance.
There are steps that can be taken to remedy this problem, such as the use of a lip liner with the high shine product, the use of a separate gloss over a matte lipstick to achieve the desired shine, or the use of various pearlescent fillers to produce a pearl-based, rather than oil-based, shine. However, the additional steps required may be unsatisfactory to some consumers, while the pearlescent shine may not be as appealing to some users as the oil-based shine.
An alternative solution is the use of controlled release materials. These materials, typically solids containing entrapped or adsorbed liquids, which act as the shine component, are applied to the lip. The liquid is released by shear force (i.e., by the force of application) or by the ultimate force of 3o equilibrium conditions, giving a glossy appearance for a period of time.
However, to date, these technologies have not yielded the type of super-shine product that is currently so much in demand.
Yet another possibility for producing shine is the use of film forming agents in the composition. Such materials do provide a certain level of gloss, but that gloss is proportional to the amount of film former used. Issues of comfort and aesthetics limit the amount of film forming agents that can. be used in a lip composition, so this approach has found limited success in producing a high shine product.
It has also been recognized that a combination of two or more of these approaches may yield the desired high gloss lip product. However, the combination is more easily managed in concept than in practice: achieving compatibility of film-formers, controlled release agents and other shine-boosting components to achieve high shine, while avoiding syneresis and/or reducing feathering, has not been a simple task.
There is thus still a need for a high shine cosmetic composition that avoids the unattractive feathering and short wear problems, while providing a vivid gloss to the user's lips, all in a single product. The present invention provides a solution to this need.
Summary of the Invention The invention provides cosmetic compositions comprising at least one water insoluble, fatty alcohol soluble polysaccharide polymer in combination with at least one liquid polyol ester. The compositions of the invention are particularly suitable for use in a lip product, providing a long-lasting high shine, with minimal or no feathering. The invention also provides a method of providing high shine to a keratinous surface comprising applying to the surface a composition comprising at least one water insoluble, fatty alcohol soluble carbohydrate polymer in combination with at least one liquid polyol ester.
Detailed Description of the Invention The compositions of the invention comprise two basic components, a water insoluble, fatty alcohol soluble polysaccharide polymer blended with a liquid polyol ester. The combination of these two types of molecules results in a softly gelled system which, when applied to the skin, slowly releases the ester (the shine component), resulting in a longer lasting shine that has typically been achieved with other high shine cosmetics which have relied on shine from film formers or oils.
The polysaccharide polymer employed in the invention is one that is capable of gelling an oil phase, particularly a polar oil phase. The ideal polymer is one which is substantially water insoluble, but is fatty alcohol soluble. Examples of useful categories of polysaccharides are water insoluble, fatty alcohol soluble starches, glycogens, dextrins and celluloses.
Particularly useful are water insoluble, fatty alcohol soluble celluloses, in 1o particular C1-C8 alkyl-modified celluloses. In a preferred embodiment, the polymer is an ethyl cellulose. Ethyl celluloses are widely used in both cosmetic and pharmaceutical formulations, as film formers, binders, fillers, and delayed release systems. Any water-insoluble ethyl cellulose, or combinations thereof, is appropriate for use in the present invention.
1s Particularly preferred, however, are ethyl celluloses routinely used for microencapsulation purposes. Examples of such ethylcelluloses are those sold by Dow Chemical Company under the brand name Ethocel. , Standard 45 Premium, which has a number average molecular weight (Mn) of about 15,000 and a weight average molecular weight (Mw) of about 160,000, or 20 Ethocel , Standard 100 Premium, with an Mn of about 20,000 and Mw of about 220,000. Other equivalent ethylcelluloses are also commercially available, such as AqualonTM and NatrosolTM grades cellulose (Aqualon Company) and Stabilizer (TIC Gums). A preferred embodiment is one in which Ethocel Standard 45 is combined with Ethocel Standard 100, in 'a ratio of 25 about 1.5:1. The quantities of polysaccharide polymer to be used will depend upon the desired viscosity of the final product, and thus will be a matter of choice for the user. However, as a guideline, the amount will ordinarily be from about 0.1 to about 20.0 % by weight of the total composition, preferably about 0.5 to about 10.0%, and more preferably about 1 to about 5%.
30 The polysaccharide polymer is used in combination with at least one liquid polyol ester base, which serves as the primary shine component of the composition. The esters of interest are relatively polar solvents/ emollients that are known in the art, as described, for example, in GB 2,134,538, JP 5-120209, and US 3,694,382.
The esters of interest are the products of esterification of a polyol, a monocarboxylic acid and a dicarboxylic acid, such as described. in the above-referenced patent documents and WO 93/25628.
The polyol component of these esters is a C2-20 polyol, such as sugars or sugar alcohols, for example xylose, xylitol, erythritol, sucrose, glucose, maltose, lactose, sorbose, sorbitol, lactitol or maltitol, and derivatives thereof. Particularly useful polyols include, but are not limited to, glycerol, pentaerythritol, dipentaerythritol, tripentaerythritol, trimethylol propane, neopentyl glycol or combinations thereof.
The monocarboxylic acid component is a C4-30 carboxylic acid, which may be branched, straight chain or aromatic, or any mixture thereof.
Preferably, the monocarboxylic acid is a C6-C22 monocarboxylic acid, or combinations thereof. Examples of such monocarboxylic acids are stearic, caprylic, capric, myristic, lauric, linoleic, oleic, linolenic, arachidic, arachidonic, erucic, ricinoleic, palmitic, palmitoleic and behenic acids.
Particularly preferred are C6-C 12 monocarboxylic acids, such as caprylic or capric, or combinations thereof.
The dicarboxylic acid component of the polyol ester may be any C2-36 straight chain, branched chain, cyclic dicarboxylic acids, or dieters of monocarboxylic fatty acids (e.g., dilinoleic acid) or combinations thereof.
Preferably, a C4-C 10 dicarboxylic acid, or combination thereof, is used. More preferably, the dicarboxylic acid is selected from adipic acid, succinic acid, or heptandioic acid.
As noted above, these liquid polyols, and methods of making same, are well known in the art. They are also widely commercially available.
Such products can be purchased under the commercial names of PuresynTM
(e.g., PuresynTM ME450, with a viscosity of 220cPs at 25 C, and ME100, with a viscosity of about 1050 cPS at 25 C from Exxon-Mobil Chemical). A
particularly preferred polyol is a pentaerythrityl adipate/caprate/caprylate/heptanoate purchased from Inolex, under the trade name LexfeelTM EL500. The amount of polyol employed in the composition is from about 5 to about 90% by weight of the composition, preferably from about 10 to about 75%, and more preferably about 30 to about 60%.
Although the polysaccaride polymer and the liquid polyol can be used alone in the composition, it is more often preferred to provide additional components to optimize function or for aesthetic reasons. One particularly preferred additional component is one or more fatty alcohols.
The fatty alcohol increases the compatibility of the polysaccharide with the polyol, enhancing its solubility therein, and also provides to additional emolliency to the product. The fatty alcohols used in the composition can be any C4-C36 fatty alcohol, preferably a C4-C22 fatty alcohol, and more preferably a C12-C22 alcohol, or any combination thereof.
A particularly preferred fatty alcohol is octyldodecanol, used either alone, or in combination with another fatty alcohol. For example, octyldodecanol can be combined with a dimer fatty alcohol to increase its viscosity. A preferred dimer alcohol is a C 18 dimer alcohol. The fatty alcohols are employed in an amount of from about 2 to about 80%, preferably about 5 to about 60%, and more preferably about 10 to about 30%, by weight of the. composition.
Although fatty alcohols are incorporated to enhance compatibility of the polysaccride with the polyol, it is not necessary, nor even desirable, to have complete compatibility/ solubility of these two components.
The objective is to achieve sufficient compatibility such that the product holds together as a single phase at least until the time of application, but not so much as to prevent their separation under the high shear conditions of application to a keratinous surface such as skin. While not wishing to be bound by any theory, it is believed that when mixed, the polysaccharide polymer may "microencapsulate"- the polyol ester, providing a single homogeneous phase as a final product, but when applied to, for example, the lips, the encapsulation is disrupted by the shear force of the application process, gradually releasing the polyol ester, and thus providing a longer lasting shine. An added benefit of the composition, in the use of a polyol ester, is that, by virtue of its polarity, it has a relatively high surface tension, causing it to bead up on a lower-polarity or non-polar substrate, which has lower surface tension. Thus, the relatively polar esters, when released onto the lip, will not have as great a tendency to migrate, and will not spread much, if at all, beyond the edge of the applied film, thereby reducing feathering substantially. The use of the fatty alcohol, also relatively polar in comparison with other emollients, also reduces the capillary effect that is a major contributor to bleeding or feathering.
Although fatty alcohols are the preferred means for increasing the polysaccharide's compatibility with the ester, alternate components can also be used, either alone, or as a supplement to the fatty alcohol. If additional emolliency is desired, it may be advantageous to incorporate other polar emollients, such as liquid fatty acids (e.g., isostearic acid), or relatively polar liquid non-polymeric fatty acid esters, typically up to C18, for example neopentyl glycol diheptanoate, alkyl isononanoate, alkyl palmitate, or myristyl octanoate; esters having a free hydroxy group, such as ethyl hexyl hydroxy stearate, octyl hydroxystearate, or glyceryl mono and/or dialkyl esters; or polar vegetable oils and/or triglycerides, such as caprylic/capric triglyceride; and any mixture of the relatively polar components. Such materials not only add to the emolliency of the product, but as liquids, can also aid in improving the solubility of the polysaccharide in the ester. The amounts of these materials, if used, can be in the same range as the fatty alcohols, as described above. However, particularly with regard to fatty acids, it is possible to achieve the desired effect with relatively small amounts, e.g., in about a 1:1 ratio with the polysaccharide. Larger quantities can be employed, but with fatty acids, it is preferable to keep the amounts low due to possible irritation, but with higher amounts, this can also be countered by adding to the product an antiirritant component.
Other optional components may be incorporated, depending on the intended end use and/or form of the product. As noted above, one of the preferred and advantageous uses of the compositions is as a lip product. In this regard, the product as described above can provide a soft gel which is fully functional as a high shine lip product. However, in order to obtain a more solid product, for example, to achieve a soft stick consistency, it may be desired to add to the composition one or more thickeners and/or structuring agents. Because retaining the overall relative polarity of the composition is important to the desired performance, it is preferred not to utilize large quantities of the non-polar compounds that are traditionally utilized for structuring or thickening stick products. However, small amounts, preferably no more than 2 5% by weight, of such materials, for example hydrocarbon waxes, petrolatum, silicone-based resins or elastomers, or hydrocarbon polymers, such as linear or branched polybutene, polyisobutene, polyethylene, polydecene, hydrogenated derivatives thereof, and copolymers thereof, ethoxylated alcohols, or bentones, and any mixtures of the foregoing, can be employed to enhance the structure, viscosity and/or feel of the final product.
In a particularly preferred embodiment, however, a.gelling system is used that is particularly adapted for thickening of polar oils. An example of such a system is the combination of at least one silica and at least one sugar fatty acid ester or ether, such as described in copending US Patent Publication No. 2005-0112161, published May 26, 2005.
Any silica particle can be used in the combination, provided the particle is not fully surface-coated. Use of partially coated products, while possible, will result in the need to use higher levels of silica to achieve the desired effect. If used in the composition, the amount can be up to- about 40% by weight of the composition, but more typically the amount will be from about 0.1 to about 30%, preferably about .5 to about 10%, more preferably about 1 to about 5%, by weight of the Any type of silica, or any combination of types of silica, can be used, but the silica is preferably not completely surface coated.
A particularly useful silica is a fumed silica commercially available from Cabot Corporation under the trade name Cab-O-SilTM M-5.
The sugar fatty acid ester employed in the invention is a compound obtained by reacting a saturated or unsaturated C12-C22 fatty acid, preferably C16-C20 carbon atoms with a sugar or alkylsugar in which the 3o alkyl group contains from 1 to 8 carbon atoms. The sugar is preferably a mono- or oligosaccharide. Examples of useful mono- or oligosaccharides include, but are not limited to, glucose, sucrose, galactose, fructose, lactose, mannose, maltose, trehalose, melibiose, raffinose, or ribose. A preferred sugar fatty ester is a fatty ester of glucose or alkylglucose. The fatty acid esters of alkylglucose are ethers of glucose in which the alkyl chain comprises from 1 to 8 carbon, atoms, preferably 1-4 carbon atoms. The preferred ester may contain a mixture of mono-, di-, tri- and tetraester derivatives with a proportion which may be of at least 50% by weight of mono- and diester derivatives and usually not exceeding 95% by weight of monoester derivatives relative to the total weight of the mixture. Examples of sugar fatty esters that may be used in the invention include, but are not limited to, sucrose monolaurate, glucose palmitate, alkylglucose sesquistearates, for instance methylglucose sesquistearate and alkylglucose palmitates, for instance methylglucose palmitate or ethylglucose palmitate, as well as the PEG or PPG derivatives of such compounds, for example, PEG-methyl glucose sesquistearate. Such compounds are widely available commercially, e.g., under the tradenames GlucateTM, GlucamTM, and 15 GlucamateTM (Amerchol), GrillocoseTM (Grillo-Werke), and AntilTM(Goldschmidt). The amount of ester used in the composition will be from about 0.1 to about 10%, preferably about 0.5 to about 5%, by weight of the composition.
The viscosity of the end product is dependent upon the ratio of the 20 amount of silica to the amount of sugar fatty acid ester. Overall the ratio of these materials will range from about 10:0.5 to 0.5:5.0 silica to ester, with the lower amounts of the silica producing a lower viscosity product, and higher amounts of the silica producing a higher viscosity product. A product having a ratio of about 4.0:1.0 -1:1, preferably about 2:1-1:1, silica: ester is particularly preferred. The viscosity is also ultimately affected by the amount of gellant used relative to the amount of polar oil, with a higher viscosity achieved by a higher amount of gelling components. The viscosity is also affected by the polarity of the oils used, as the silica is more readily suspended in a more polar oil, presumably due to the interaction of the 3o hydroxyl groups of the silica and the polar groups on the oils, so that a well-suspended silica can be used at smaller amounts than a silica that is not so readily suspended.
Field of the Invention The invention relates to cosmetic compositions. In particular, the invention relates to color cosmetics, particularly lip products.
Background of the Invention Lip products come in a variety of forms, which vary depending upon the look desired by the user. The products may be highly pigmented, pearlescent, matte, or glossy/shiny. The latter type, i.e., the high gloss type of lip color, is currently particularly popular, especially among young women.
The look conferred by such a product is highly glamorous and sensual, but has several drawbacks associated with it. The current technology available to produce a high shine lipstick is such that those lipstick or glosses giving the best shine typically have little staying power on the lips. In addition, these products also give rise to moderate to severe feathering, a condition in which the pigment intended to color the lips actually migrates into the fine lines around the mouth, producing a smeared, unattractive appearance.
There are steps that can be taken to remedy this problem, such as the use of a lip liner with the high shine product, the use of a separate gloss over a matte lipstick to achieve the desired shine, or the use of various pearlescent fillers to produce a pearl-based, rather than oil-based, shine. However, the additional steps required may be unsatisfactory to some consumers, while the pearlescent shine may not be as appealing to some users as the oil-based shine.
An alternative solution is the use of controlled release materials. These materials, typically solids containing entrapped or adsorbed liquids, which act as the shine component, are applied to the lip. The liquid is released by shear force (i.e., by the force of application) or by the ultimate force of 3o equilibrium conditions, giving a glossy appearance for a period of time.
However, to date, these technologies have not yielded the type of super-shine product that is currently so much in demand.
Yet another possibility for producing shine is the use of film forming agents in the composition. Such materials do provide a certain level of gloss, but that gloss is proportional to the amount of film former used. Issues of comfort and aesthetics limit the amount of film forming agents that can. be used in a lip composition, so this approach has found limited success in producing a high shine product.
It has also been recognized that a combination of two or more of these approaches may yield the desired high gloss lip product. However, the combination is more easily managed in concept than in practice: achieving compatibility of film-formers, controlled release agents and other shine-boosting components to achieve high shine, while avoiding syneresis and/or reducing feathering, has not been a simple task.
There is thus still a need for a high shine cosmetic composition that avoids the unattractive feathering and short wear problems, while providing a vivid gloss to the user's lips, all in a single product. The present invention provides a solution to this need.
Summary of the Invention The invention provides cosmetic compositions comprising at least one water insoluble, fatty alcohol soluble polysaccharide polymer in combination with at least one liquid polyol ester. The compositions of the invention are particularly suitable for use in a lip product, providing a long-lasting high shine, with minimal or no feathering. The invention also provides a method of providing high shine to a keratinous surface comprising applying to the surface a composition comprising at least one water insoluble, fatty alcohol soluble carbohydrate polymer in combination with at least one liquid polyol ester.
Detailed Description of the Invention The compositions of the invention comprise two basic components, a water insoluble, fatty alcohol soluble polysaccharide polymer blended with a liquid polyol ester. The combination of these two types of molecules results in a softly gelled system which, when applied to the skin, slowly releases the ester (the shine component), resulting in a longer lasting shine that has typically been achieved with other high shine cosmetics which have relied on shine from film formers or oils.
The polysaccharide polymer employed in the invention is one that is capable of gelling an oil phase, particularly a polar oil phase. The ideal polymer is one which is substantially water insoluble, but is fatty alcohol soluble. Examples of useful categories of polysaccharides are water insoluble, fatty alcohol soluble starches, glycogens, dextrins and celluloses.
Particularly useful are water insoluble, fatty alcohol soluble celluloses, in 1o particular C1-C8 alkyl-modified celluloses. In a preferred embodiment, the polymer is an ethyl cellulose. Ethyl celluloses are widely used in both cosmetic and pharmaceutical formulations, as film formers, binders, fillers, and delayed release systems. Any water-insoluble ethyl cellulose, or combinations thereof, is appropriate for use in the present invention.
1s Particularly preferred, however, are ethyl celluloses routinely used for microencapsulation purposes. Examples of such ethylcelluloses are those sold by Dow Chemical Company under the brand name Ethocel. , Standard 45 Premium, which has a number average molecular weight (Mn) of about 15,000 and a weight average molecular weight (Mw) of about 160,000, or 20 Ethocel , Standard 100 Premium, with an Mn of about 20,000 and Mw of about 220,000. Other equivalent ethylcelluloses are also commercially available, such as AqualonTM and NatrosolTM grades cellulose (Aqualon Company) and Stabilizer (TIC Gums). A preferred embodiment is one in which Ethocel Standard 45 is combined with Ethocel Standard 100, in 'a ratio of 25 about 1.5:1. The quantities of polysaccharide polymer to be used will depend upon the desired viscosity of the final product, and thus will be a matter of choice for the user. However, as a guideline, the amount will ordinarily be from about 0.1 to about 20.0 % by weight of the total composition, preferably about 0.5 to about 10.0%, and more preferably about 1 to about 5%.
30 The polysaccharide polymer is used in combination with at least one liquid polyol ester base, which serves as the primary shine component of the composition. The esters of interest are relatively polar solvents/ emollients that are known in the art, as described, for example, in GB 2,134,538, JP 5-120209, and US 3,694,382.
The esters of interest are the products of esterification of a polyol, a monocarboxylic acid and a dicarboxylic acid, such as described. in the above-referenced patent documents and WO 93/25628.
The polyol component of these esters is a C2-20 polyol, such as sugars or sugar alcohols, for example xylose, xylitol, erythritol, sucrose, glucose, maltose, lactose, sorbose, sorbitol, lactitol or maltitol, and derivatives thereof. Particularly useful polyols include, but are not limited to, glycerol, pentaerythritol, dipentaerythritol, tripentaerythritol, trimethylol propane, neopentyl glycol or combinations thereof.
The monocarboxylic acid component is a C4-30 carboxylic acid, which may be branched, straight chain or aromatic, or any mixture thereof.
Preferably, the monocarboxylic acid is a C6-C22 monocarboxylic acid, or combinations thereof. Examples of such monocarboxylic acids are stearic, caprylic, capric, myristic, lauric, linoleic, oleic, linolenic, arachidic, arachidonic, erucic, ricinoleic, palmitic, palmitoleic and behenic acids.
Particularly preferred are C6-C 12 monocarboxylic acids, such as caprylic or capric, or combinations thereof.
The dicarboxylic acid component of the polyol ester may be any C2-36 straight chain, branched chain, cyclic dicarboxylic acids, or dieters of monocarboxylic fatty acids (e.g., dilinoleic acid) or combinations thereof.
Preferably, a C4-C 10 dicarboxylic acid, or combination thereof, is used. More preferably, the dicarboxylic acid is selected from adipic acid, succinic acid, or heptandioic acid.
As noted above, these liquid polyols, and methods of making same, are well known in the art. They are also widely commercially available.
Such products can be purchased under the commercial names of PuresynTM
(e.g., PuresynTM ME450, with a viscosity of 220cPs at 25 C, and ME100, with a viscosity of about 1050 cPS at 25 C from Exxon-Mobil Chemical). A
particularly preferred polyol is a pentaerythrityl adipate/caprate/caprylate/heptanoate purchased from Inolex, under the trade name LexfeelTM EL500. The amount of polyol employed in the composition is from about 5 to about 90% by weight of the composition, preferably from about 10 to about 75%, and more preferably about 30 to about 60%.
Although the polysaccaride polymer and the liquid polyol can be used alone in the composition, it is more often preferred to provide additional components to optimize function or for aesthetic reasons. One particularly preferred additional component is one or more fatty alcohols.
The fatty alcohol increases the compatibility of the polysaccharide with the polyol, enhancing its solubility therein, and also provides to additional emolliency to the product. The fatty alcohols used in the composition can be any C4-C36 fatty alcohol, preferably a C4-C22 fatty alcohol, and more preferably a C12-C22 alcohol, or any combination thereof.
A particularly preferred fatty alcohol is octyldodecanol, used either alone, or in combination with another fatty alcohol. For example, octyldodecanol can be combined with a dimer fatty alcohol to increase its viscosity. A preferred dimer alcohol is a C 18 dimer alcohol. The fatty alcohols are employed in an amount of from about 2 to about 80%, preferably about 5 to about 60%, and more preferably about 10 to about 30%, by weight of the. composition.
Although fatty alcohols are incorporated to enhance compatibility of the polysaccride with the polyol, it is not necessary, nor even desirable, to have complete compatibility/ solubility of these two components.
The objective is to achieve sufficient compatibility such that the product holds together as a single phase at least until the time of application, but not so much as to prevent their separation under the high shear conditions of application to a keratinous surface such as skin. While not wishing to be bound by any theory, it is believed that when mixed, the polysaccharide polymer may "microencapsulate"- the polyol ester, providing a single homogeneous phase as a final product, but when applied to, for example, the lips, the encapsulation is disrupted by the shear force of the application process, gradually releasing the polyol ester, and thus providing a longer lasting shine. An added benefit of the composition, in the use of a polyol ester, is that, by virtue of its polarity, it has a relatively high surface tension, causing it to bead up on a lower-polarity or non-polar substrate, which has lower surface tension. Thus, the relatively polar esters, when released onto the lip, will not have as great a tendency to migrate, and will not spread much, if at all, beyond the edge of the applied film, thereby reducing feathering substantially. The use of the fatty alcohol, also relatively polar in comparison with other emollients, also reduces the capillary effect that is a major contributor to bleeding or feathering.
Although fatty alcohols are the preferred means for increasing the polysaccharide's compatibility with the ester, alternate components can also be used, either alone, or as a supplement to the fatty alcohol. If additional emolliency is desired, it may be advantageous to incorporate other polar emollients, such as liquid fatty acids (e.g., isostearic acid), or relatively polar liquid non-polymeric fatty acid esters, typically up to C18, for example neopentyl glycol diheptanoate, alkyl isononanoate, alkyl palmitate, or myristyl octanoate; esters having a free hydroxy group, such as ethyl hexyl hydroxy stearate, octyl hydroxystearate, or glyceryl mono and/or dialkyl esters; or polar vegetable oils and/or triglycerides, such as caprylic/capric triglyceride; and any mixture of the relatively polar components. Such materials not only add to the emolliency of the product, but as liquids, can also aid in improving the solubility of the polysaccharide in the ester. The amounts of these materials, if used, can be in the same range as the fatty alcohols, as described above. However, particularly with regard to fatty acids, it is possible to achieve the desired effect with relatively small amounts, e.g., in about a 1:1 ratio with the polysaccharide. Larger quantities can be employed, but with fatty acids, it is preferable to keep the amounts low due to possible irritation, but with higher amounts, this can also be countered by adding to the product an antiirritant component.
Other optional components may be incorporated, depending on the intended end use and/or form of the product. As noted above, one of the preferred and advantageous uses of the compositions is as a lip product. In this regard, the product as described above can provide a soft gel which is fully functional as a high shine lip product. However, in order to obtain a more solid product, for example, to achieve a soft stick consistency, it may be desired to add to the composition one or more thickeners and/or structuring agents. Because retaining the overall relative polarity of the composition is important to the desired performance, it is preferred not to utilize large quantities of the non-polar compounds that are traditionally utilized for structuring or thickening stick products. However, small amounts, preferably no more than 2 5% by weight, of such materials, for example hydrocarbon waxes, petrolatum, silicone-based resins or elastomers, or hydrocarbon polymers, such as linear or branched polybutene, polyisobutene, polyethylene, polydecene, hydrogenated derivatives thereof, and copolymers thereof, ethoxylated alcohols, or bentones, and any mixtures of the foregoing, can be employed to enhance the structure, viscosity and/or feel of the final product.
In a particularly preferred embodiment, however, a.gelling system is used that is particularly adapted for thickening of polar oils. An example of such a system is the combination of at least one silica and at least one sugar fatty acid ester or ether, such as described in copending US Patent Publication No. 2005-0112161, published May 26, 2005.
Any silica particle can be used in the combination, provided the particle is not fully surface-coated. Use of partially coated products, while possible, will result in the need to use higher levels of silica to achieve the desired effect. If used in the composition, the amount can be up to- about 40% by weight of the composition, but more typically the amount will be from about 0.1 to about 30%, preferably about .5 to about 10%, more preferably about 1 to about 5%, by weight of the Any type of silica, or any combination of types of silica, can be used, but the silica is preferably not completely surface coated.
A particularly useful silica is a fumed silica commercially available from Cabot Corporation under the trade name Cab-O-SilTM M-5.
The sugar fatty acid ester employed in the invention is a compound obtained by reacting a saturated or unsaturated C12-C22 fatty acid, preferably C16-C20 carbon atoms with a sugar or alkylsugar in which the 3o alkyl group contains from 1 to 8 carbon atoms. The sugar is preferably a mono- or oligosaccharide. Examples of useful mono- or oligosaccharides include, but are not limited to, glucose, sucrose, galactose, fructose, lactose, mannose, maltose, trehalose, melibiose, raffinose, or ribose. A preferred sugar fatty ester is a fatty ester of glucose or alkylglucose. The fatty acid esters of alkylglucose are ethers of glucose in which the alkyl chain comprises from 1 to 8 carbon, atoms, preferably 1-4 carbon atoms. The preferred ester may contain a mixture of mono-, di-, tri- and tetraester derivatives with a proportion which may be of at least 50% by weight of mono- and diester derivatives and usually not exceeding 95% by weight of monoester derivatives relative to the total weight of the mixture. Examples of sugar fatty esters that may be used in the invention include, but are not limited to, sucrose monolaurate, glucose palmitate, alkylglucose sesquistearates, for instance methylglucose sesquistearate and alkylglucose palmitates, for instance methylglucose palmitate or ethylglucose palmitate, as well as the PEG or PPG derivatives of such compounds, for example, PEG-methyl glucose sesquistearate. Such compounds are widely available commercially, e.g., under the tradenames GlucateTM, GlucamTM, and 15 GlucamateTM (Amerchol), GrillocoseTM (Grillo-Werke), and AntilTM(Goldschmidt). The amount of ester used in the composition will be from about 0.1 to about 10%, preferably about 0.5 to about 5%, by weight of the composition.
The viscosity of the end product is dependent upon the ratio of the 20 amount of silica to the amount of sugar fatty acid ester. Overall the ratio of these materials will range from about 10:0.5 to 0.5:5.0 silica to ester, with the lower amounts of the silica producing a lower viscosity product, and higher amounts of the silica producing a higher viscosity product. A product having a ratio of about 4.0:1.0 -1:1, preferably about 2:1-1:1, silica: ester is particularly preferred. The viscosity is also ultimately affected by the amount of gellant used relative to the amount of polar oil, with a higher viscosity achieved by a higher amount of gelling components. The viscosity is also affected by the polarity of the oils used, as the silica is more readily suspended in a more polar oil, presumably due to the interaction of the 3o hydroxyl groups of the silica and the polar groups on the oils, so that a well-suspended silica can be used at smaller amounts than a silica that is not so readily suspended.
In one optional embodiment, it is possible to increase even further the lasting shine produced by the foregoing by adding to the composition one or more beads or resin particles having a coarse, rough or porous surface, and/or= hollow internal cavity, which can hold any of the liquids until the high shear of application causes the liquid to be released. A particularly useful particle for this purpose is Silica MSS500/3H (Lobo). Although not in any way essential to achieve the desired high shine, such particles do appear to prolong the effect, presumably by their delayed release of emollients that contribute to the shine. Amounts, if used, are not critical, and will ordinarily be used in an amount of about .05 to about 5%.
Another optional ingredient for contributing to the prolonged appearance of the desired shine is a low-melting point resin or butter. By low-melting point is meant a material that melts at about normal human body temperature, so that upon application to the skin, the material gradually melts, releasing, in its liquid form, yet another source of shine.
One example of such a material is stearoxy methicone/dimethicone copolymer, sold under the commercial name of GransilTM ST-9 (Grant Industries).
If the product is to be used as a color cosmetic, it will also contain one or more pigments or colorants. Any type of pigment, provided it is acceptable for use in the area to which the product will be applied, and with or without surface treatment, can be used in the product of the invention: examples of useful pigments include iron oxides (yellow, red, brown or black), titanium dioxide (white), zinc oxide, chrome oxide (green), chrome hydrate (green), ultramarines, manganese violet, ferric ferrocyanide, carmine 40, ferric ammonium ferrocyanide, or combinations thereof. Interference pigments, which are thin platelike layered particles having a high refractive index, which, at a certain thickness, produce interference colors, resulting from the interference of typically two, but occasionally more, light reflections, from 3o different layers of the plate, can also be added to provide a pearlescence to' the product, is such is desired. The composition may also contain one or more types of cosmetically acceptable glitter, i.e., particles of transparent or colored, solid organic materials, such as poly (ethylene terephthalate), polymethacrylate, and poly (vinylbutyral), particles of metal, or particles of metal coated film or paper.
Organic pigments may also optionally be included; these include natural colorants and synthetic monomeric and polymeric colorants.
Exemplary are phthalocyanine blue and green pigment, diarylide yellow and orange pigments, and azo-type red and yellow pigments such as toluidine red, litho red, naphthol red and brown pigments. Also useful are lakes, which are pigments formed by the precipitation and absorption of organic dyes on an insoluble base, such as alumina, barium, or calcium hydrates.
Particularly preferred lakes are primary FD&C or D&C Lakes and blends thereof. Stains, such as bromo dyes and fluorescein dyes can also be employed. Pigments when used are typically present in an amount of about .1 to about 30%, preferably about 0.1 to about 20%, by weight of the composition.
The compositions can also contain inorganic powders, such as soft focus powders, or plate- like non-spherical powders such as bismuth oxychloride, boron nitride, barium sulfate, mica, sericite, muscovite, synthetic mica, titanium oxide coated mica, titanium oxide-coated bismuth oxychloride, titanium oxide coated talc, platelet iron oxides, metal powders such as aluminum, lauroyl lysine and platelet talc. Amounts are not critical, but if used, typically will be used in an amount of about 0.5 to about 5%
The composition may also contain oil soluble active agents and skin conditioning agents. Non-limiting examples of these materials include antioxidants, ceramides, fatty acids, sunscreens, oil soluble vitamins and plant extracts, and the like. Although the most preferred embodiment of the invention is an anhydrous composition, it is possible to utilize the compositions of the invention as the oil-phase of a water and oil emulsion.
When used as the oil phase of an emulsion, the composition's water phase can also contain water soluble actives.
The compositions of the invention can be used in any situation in which it is desirable to confer shine to. a keratinous surface. A particularly preferred use is as a lip product, such as a lipstick, gloss, gel, or balm.
However, it may also be used, either as any other type of cosmetic, with or without color, where a shine is wanted, for example, a foundation, blush, eyeshadow, eyeliner, mascara, body paint, body makeup or bronzer, or as in a skin care product, such as a sunscreen, moisturizer, or self-tanner, for application to the face or body. It can also be used in hair care or styling products, so as to add a shiny appearance to hair. In addition to the shine provided on the surfaces to which they are applied, these compositions also provides a moisturizing effect, particularly when applied to the lips.
The invention is illustrated by the following. non-limiting examples.
Example 1.
This illustrates a formula of the present invention Sequence Material Weight percent 1 Ethylcellulose 0.624 (Dow Chemical Ethocel Standard 100 Premium) Ethylcellulose 0.936 (Dow Chemical Ethocel Standard 45 Premium) Pentaerythrityl adipate/ 4.94 caprate / caprylate / heptano ate (LexfeelTM EL500) Octyldodecanol 2.60 Hydrogenated dilinoleyl alcohol 3.90 2 Silica (MSS-500/3H) 3.00 Octyldodecanol 12.00 3 Silica (Cab-o-SilTM M5) 0.50 Octyldodecanol 4.50 4 Polyethylene 5.25 (PerformaleneTM 400) C20-40 Pareth-10 0.50 Microcrystalline wax 2.50 Stearoxymethicone / dimethicone 5.00 cross of er Lauryl PCA 0.50 Polybutene 2.50 Hydrogenated dilinoleyl alcohol 2.00 Propylparaben 0.10 BHT 0.05 Tocopheryl acetate 0.10 Bis-diglyceryl polyacyladipate-2 7.49 Ceramide 3 0.05 Oleic acid 0.02 Cholesterol 0.03 6 Penterythrityl/adipate/ 27.792 Ca rate ca late he tanoate Cetyl PEG/PPG-10/ 1 dimethicone// 0.164 Pol l ce l-4 isostearate he l laurate Pigment 4. 934 7 Pigment 7.23 8 Methyl glucose sesquistearate 0.790 To make a one kilogram batch, the ethylcellulose polymers (Sequence 1) are added into the premixed emollients and other liquids, and mixed well at room temperature. The system temperature is then raised to about 90-5 95 C with 100-400 rpm mixing speed until a clear viscous soft gel is formed.
In two separate vessels, the two silicas (Sequences 2 and 3) are combined with the octyldocecanol and homogenized until smooth.
Sequences 1, 2 and 3, and all other sequences except pigments and powders, are combined in a 2 liter beaker, mixed at 92-98 C, with a speed of 1o about 100-250rpm until all materials are dissolved.
Sequence 6 is added to the system, which continues to be mixed until smooth.
Sequence 7 is then added and mixed until all are mixed in.
Sequence 8 is then added, and the system kept under the same conditions for at least 30 minutes, then cooled down to about 85-90 C for pouring.
Another optional ingredient for contributing to the prolonged appearance of the desired shine is a low-melting point resin or butter. By low-melting point is meant a material that melts at about normal human body temperature, so that upon application to the skin, the material gradually melts, releasing, in its liquid form, yet another source of shine.
One example of such a material is stearoxy methicone/dimethicone copolymer, sold under the commercial name of GransilTM ST-9 (Grant Industries).
If the product is to be used as a color cosmetic, it will also contain one or more pigments or colorants. Any type of pigment, provided it is acceptable for use in the area to which the product will be applied, and with or without surface treatment, can be used in the product of the invention: examples of useful pigments include iron oxides (yellow, red, brown or black), titanium dioxide (white), zinc oxide, chrome oxide (green), chrome hydrate (green), ultramarines, manganese violet, ferric ferrocyanide, carmine 40, ferric ammonium ferrocyanide, or combinations thereof. Interference pigments, which are thin platelike layered particles having a high refractive index, which, at a certain thickness, produce interference colors, resulting from the interference of typically two, but occasionally more, light reflections, from 3o different layers of the plate, can also be added to provide a pearlescence to' the product, is such is desired. The composition may also contain one or more types of cosmetically acceptable glitter, i.e., particles of transparent or colored, solid organic materials, such as poly (ethylene terephthalate), polymethacrylate, and poly (vinylbutyral), particles of metal, or particles of metal coated film or paper.
Organic pigments may also optionally be included; these include natural colorants and synthetic monomeric and polymeric colorants.
Exemplary are phthalocyanine blue and green pigment, diarylide yellow and orange pigments, and azo-type red and yellow pigments such as toluidine red, litho red, naphthol red and brown pigments. Also useful are lakes, which are pigments formed by the precipitation and absorption of organic dyes on an insoluble base, such as alumina, barium, or calcium hydrates.
Particularly preferred lakes are primary FD&C or D&C Lakes and blends thereof. Stains, such as bromo dyes and fluorescein dyes can also be employed. Pigments when used are typically present in an amount of about .1 to about 30%, preferably about 0.1 to about 20%, by weight of the composition.
The compositions can also contain inorganic powders, such as soft focus powders, or plate- like non-spherical powders such as bismuth oxychloride, boron nitride, barium sulfate, mica, sericite, muscovite, synthetic mica, titanium oxide coated mica, titanium oxide-coated bismuth oxychloride, titanium oxide coated talc, platelet iron oxides, metal powders such as aluminum, lauroyl lysine and platelet talc. Amounts are not critical, but if used, typically will be used in an amount of about 0.5 to about 5%
The composition may also contain oil soluble active agents and skin conditioning agents. Non-limiting examples of these materials include antioxidants, ceramides, fatty acids, sunscreens, oil soluble vitamins and plant extracts, and the like. Although the most preferred embodiment of the invention is an anhydrous composition, it is possible to utilize the compositions of the invention as the oil-phase of a water and oil emulsion.
When used as the oil phase of an emulsion, the composition's water phase can also contain water soluble actives.
The compositions of the invention can be used in any situation in which it is desirable to confer shine to. a keratinous surface. A particularly preferred use is as a lip product, such as a lipstick, gloss, gel, or balm.
However, it may also be used, either as any other type of cosmetic, with or without color, where a shine is wanted, for example, a foundation, blush, eyeshadow, eyeliner, mascara, body paint, body makeup or bronzer, or as in a skin care product, such as a sunscreen, moisturizer, or self-tanner, for application to the face or body. It can also be used in hair care or styling products, so as to add a shiny appearance to hair. In addition to the shine provided on the surfaces to which they are applied, these compositions also provides a moisturizing effect, particularly when applied to the lips.
The invention is illustrated by the following. non-limiting examples.
Example 1.
This illustrates a formula of the present invention Sequence Material Weight percent 1 Ethylcellulose 0.624 (Dow Chemical Ethocel Standard 100 Premium) Ethylcellulose 0.936 (Dow Chemical Ethocel Standard 45 Premium) Pentaerythrityl adipate/ 4.94 caprate / caprylate / heptano ate (LexfeelTM EL500) Octyldodecanol 2.60 Hydrogenated dilinoleyl alcohol 3.90 2 Silica (MSS-500/3H) 3.00 Octyldodecanol 12.00 3 Silica (Cab-o-SilTM M5) 0.50 Octyldodecanol 4.50 4 Polyethylene 5.25 (PerformaleneTM 400) C20-40 Pareth-10 0.50 Microcrystalline wax 2.50 Stearoxymethicone / dimethicone 5.00 cross of er Lauryl PCA 0.50 Polybutene 2.50 Hydrogenated dilinoleyl alcohol 2.00 Propylparaben 0.10 BHT 0.05 Tocopheryl acetate 0.10 Bis-diglyceryl polyacyladipate-2 7.49 Ceramide 3 0.05 Oleic acid 0.02 Cholesterol 0.03 6 Penterythrityl/adipate/ 27.792 Ca rate ca late he tanoate Cetyl PEG/PPG-10/ 1 dimethicone// 0.164 Pol l ce l-4 isostearate he l laurate Pigment 4. 934 7 Pigment 7.23 8 Methyl glucose sesquistearate 0.790 To make a one kilogram batch, the ethylcellulose polymers (Sequence 1) are added into the premixed emollients and other liquids, and mixed well at room temperature. The system temperature is then raised to about 90-5 95 C with 100-400 rpm mixing speed until a clear viscous soft gel is formed.
In two separate vessels, the two silicas (Sequences 2 and 3) are combined with the octyldocecanol and homogenized until smooth.
Sequences 1, 2 and 3, and all other sequences except pigments and powders, are combined in a 2 liter beaker, mixed at 92-98 C, with a speed of 1o about 100-250rpm until all materials are dissolved.
Sequence 6 is added to the system, which continues to be mixed until smooth.
Sequence 7 is then added and mixed until all are mixed in.
Sequence 8 is then added, and the system kept under the same conditions for at least 30 minutes, then cooled down to about 85-90 C for pouring.
Claims (6)
1. A topical composition comprising at least one water-insoluble, fatty alcohol soluble ethyl cellulose, and a liquid polyol ester which is pentaerythrityl adipate/caprate/caprylate/heptanoate.
2. The composition according to claim 1 or claim 2 which also comprises a fatty alcohol.
3. The composition according to claim 1 which also comprises a polar fatty acid or a polar fatty acid ester.
4. The composition according to any one of claims 1 to 3 which comprises a gelling system comprising at least one sugar fatty acid ester or ether and at least one silica.
5. The composition of claim 4 in which the silica is a fumed silica.
6. The composition according to any one of claims 1 to 5 which also comprises a pigment or colorant.
Applications Claiming Priority (3)
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US58720904P | 2004-07-12 | 2004-07-12 | |
US60/587,209 | 2004-07-12 | ||
PCT/US2005/024416 WO2006017203A1 (en) | 2004-07-12 | 2005-07-11 | High gloss non-feathering lip product |
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Publication Number | Publication Date |
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CA2573802A1 CA2573802A1 (en) | 2006-02-16 |
CA2573802C true CA2573802C (en) | 2011-09-13 |
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CA2573802A Active CA2573802C (en) | 2004-07-12 | 2005-07-11 | High gloss, non-feathering lip product comprising a water-insoluble polysaccharide and a polyol ester |
Country Status (7)
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US (2) | US20060019848A1 (en) |
EP (1) | EP1768642A4 (en) |
JP (2) | JP2008505968A (en) |
KR (1) | KR100876264B1 (en) |
AU (1) | AU2005271921B2 (en) |
CA (1) | CA2573802C (en) |
WO (1) | WO2006017203A1 (en) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0526455D0 (en) * | 2005-12-24 | 2006-02-08 | Ici Plc | Structants for oil phases |
GB0607500D0 (en) * | 2006-04-13 | 2006-05-24 | Ici Plc | Structurants for oil phases |
US8333955B2 (en) * | 2007-03-19 | 2012-12-18 | Elc Management Llc | High shine, stick-shaped cosmetic products |
FR2921828B1 (en) * | 2007-10-04 | 2012-06-29 | Oreal | COSMETIC OR PHARMACEUTICAL COMPOSITION COMPRISING A POLYCONDENSATE, SAID POLYCONDENSATE, AND COSMETIC TREATMENT METHOD. |
FR2921831B1 (en) * | 2007-10-05 | 2014-05-09 | Oreal | COSMETIC OR DERMATOLOGICAL COMPOSITION COMPRISING A POLYMER CONTAINING JUNCTION GROUPS, AND COSMETIC PROCESSING METHOD |
WO2010068903A2 (en) * | 2008-12-11 | 2010-06-17 | L'oreal S.A. | Volumizing smudge resistant mascara composition |
FR2940069B1 (en) * | 2008-12-22 | 2011-03-18 | Oreal | COSMETIC COMPOSITION FOR MAKE-UP AND / OR LIP CARE |
US20110171152A1 (en) * | 2010-01-11 | 2011-07-14 | Tabakman Tatyana R | High Shine, Stick-Shaped Cosmetic Products |
DE202010001688U1 (en) * | 2010-02-02 | 2011-06-09 | Schwan-STABILO Cosmetics GmbH & Co. KG, 90562 | Cosmetic preparation and its use |
FR2968982B1 (en) * | 2010-12-16 | 2013-08-02 | Oreal | AQUEOUS COSMETIC COMPOSITION COMPRISING ALKYLCELLULOSE AND AN ORGANOPOLYSILOXANE ELASTOMER |
CN107375019A (en) * | 2010-09-20 | 2017-11-24 | 欧莱雅 | Aqueous cosmetic composition comprising alkylcellulose |
JP5567215B2 (en) | 2010-09-20 | 2014-08-06 | ロレアル | Aqueous cosmetic composition comprising alkylcellulose |
FR2985176B1 (en) * | 2012-01-02 | 2015-05-29 | Oreal | AQUEOUS LIQUID COSMETIC COMPOSITION COMPRISING ALKYLCELLULOSE, NON-VOLATILE OILS AND AT LEAST ONE SURFACTANT |
FR2992205B1 (en) * | 2012-06-21 | 2014-10-31 | Oreal | AQUEOUS COSMETIC COMPOSITION COMPRISING ALKYLCELLULOSE, OIL, HYDROPHOBIC SILICA AEROGEL PARTICLES AND AT LEAST ONE STABILIZING AGENT |
EP2969017B1 (en) * | 2013-03-14 | 2017-06-28 | Avon Products, Inc. | Long-wearing glossy lipcolor |
US20150139921A1 (en) * | 2013-03-15 | 2015-05-21 | Avon Products, Inc. | Compositions containing titanate silicone networks |
FR3009192B1 (en) * | 2013-07-31 | 2015-09-04 | Oreal | ANHYDROUS COSMETIC COMPOSITION COMPRISING ALKYLCELLULOSE, AT LEAST ONE BRANCHED DETERRENT ESTER AND AT LEAST ONE FATTY ALCOHOL |
CN103990424B (en) * | 2014-04-23 | 2016-03-09 | 江南大学 | A kind of preparation method of microcapsules of linear dextrin embedding CLA |
FR3041531B1 (en) * | 2015-09-25 | 2018-11-09 | Oreal | LIQUID COSMETIC COMPOSITION COMPRISING A HIGH CONTENT OF NON-VOLATILE OILS, NON-IONIC SILICONE SURFACTANT AND METHOD OF TREATING LIP |
FR3045364B1 (en) * | 2015-12-21 | 2018-01-12 | L'oreal | COMPOSITION COMPRISING ALKYLCELLULOSE, INCOMPATIBLE HYDROCARBON AND SILICONE OILS, A WAX, AND METHOD FOR CARRYING OUT THE SAME |
JP6828040B2 (en) | 2015-12-21 | 2021-02-10 | ロレアル | Compositions containing alkyl cellulose and incompatible hydrocarbons and silicone oils and methods using them |
FR3054437B1 (en) * | 2016-07-28 | 2018-09-07 | Lvmh Recherche | COSMETIC PRODUCT FOR LIQUIDS IN THE FORM OF A WATER-IN-OIL EMULSION AND METHOD OF MAKE-UP |
KR102610442B1 (en) * | 2016-09-30 | 2023-12-06 | (주)아모레퍼시픽 | Lip cosmetic compostion |
JP6910207B2 (en) * | 2017-05-26 | 2021-07-28 | 花王株式会社 | Oily cosmetics |
EP4014956A1 (en) * | 2020-12-17 | 2022-06-22 | Oleon N.V. | Transparent gel |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2051665A1 (en) * | 1969-07-10 | 1971-04-09 | Ethyl Corp | |
JPS5266637A (en) * | 1975-11-27 | 1977-06-02 | Mimatsu Kakou Kk | Cosmetics |
JPS56104807A (en) * | 1980-01-24 | 1981-08-20 | Shiseido Co Ltd | Cosmetic |
JPS59122415A (en) * | 1982-12-28 | 1984-07-14 | Kobayashi Kooc:Kk | Make-up cosmetic |
JPS606608A (en) * | 1983-06-24 | 1985-01-14 | Shiseido Co Ltd | Lipstick cosmetic |
US5093111A (en) * | 1991-03-11 | 1992-03-03 | Kolmar Laboratories Inc. | Lipstick composition comprising cetearyl isononanoate, a sesquistearate and isopropyl hydroxystearate |
JP3101035B2 (en) * | 1991-03-11 | 2000-10-23 | 株式会社コーセー | Pack cosmetics |
JPH06508625A (en) * | 1991-06-21 | 1994-09-29 | ザ ブーツ カンパニー ピーエルシー | cosmetic formulations |
CZ110796A3 (en) * | 1993-10-18 | 1996-08-14 | Procter & Gamble | Lip-sticks resistant to oil sweat-out |
FR2715063B1 (en) * | 1994-01-17 | 1996-03-22 | Oreal | Cosmetic composition for make-up in the form of a mascara containing at least one wax and one pseudo-latex of cellulose derivatives. |
US5747017A (en) * | 1995-05-15 | 1998-05-05 | Lip-Ink International | Lip cosmetic |
CA2236974C (en) * | 1995-11-07 | 2002-01-01 | The Procter & Gamble Company | Transfer resistant cosmetic compositions |
FR2746302B1 (en) * | 1996-03-20 | 1998-12-24 | Oreal | COSMETIC COMPOSITIONS COMPRISING NANOPIGMENTS |
US5667770A (en) * | 1996-03-25 | 1997-09-16 | Elizabeth Arden Company, Division Of Conopco, Inc. | Long wearing lipstick |
US5908631A (en) * | 1997-02-27 | 1999-06-01 | L'oreal S.A. | Monohydric alcohol-free composition for topical use comprising solubilized ethylcellulose |
EP0916335B1 (en) * | 1997-08-13 | 2004-11-03 | Basf Aktiengesellschaft | Cosmetic and parmaceutical compositions containing a photostable UV filter |
US6277358B1 (en) * | 1997-12-15 | 2001-08-21 | Revlon Consumer Products Corporation | Cosmetic compositions containing crosslinkable polymers |
GB9814706D0 (en) * | 1998-07-08 | 1998-09-02 | Procter & Gamble | Cleansing apparatus |
US6627586B1 (en) * | 1998-07-08 | 2003-09-30 | The Procter & Gamble Company | Cleansing compositions |
US5976514A (en) * | 1998-11-20 | 1999-11-02 | Procter & Gamble Company | Low-irritation antiperspirant and deodorant compositions containing a volatile, nonpolar hydrocarbon liquid |
JP3770583B2 (en) * | 2000-10-30 | 2006-04-26 | 株式会社コーセー | Oily cosmetics |
US20020111330A1 (en) * | 2000-12-12 | 2002-08-15 | Carlos Pinzon | Compositions containing heteropolymers and methods of using same |
US6780825B2 (en) * | 2001-02-06 | 2004-08-24 | Playtex Products, Inc. | Cleansing compositions with milk protein and aromatherapy |
US6552160B2 (en) * | 2001-05-14 | 2003-04-22 | Arizona Chemical Company | Ester-terminated poly(ester-amides) useful for formulating transparent gels in low polarity fluids |
FR2827515B1 (en) * | 2001-07-20 | 2005-06-03 | Oreal | FOAMING COMPOSITION BASED ON SILICA AND CATIONIC POLYMER |
JP2003137715A (en) * | 2001-10-29 | 2003-05-14 | Seiwa Kasei:Kk | Cosmetic |
US20040228818A1 (en) * | 2002-10-18 | 2004-11-18 | L'oreal | Cosmetic composition combining at least two dyes including at least one photochromic dye |
DE60301960T2 (en) * | 2003-08-08 | 2006-07-20 | Kpss-Kao Professional Salon Services Gmbh | Cosmetic hair composition containing cetyl PEG / PPG-10/1 dimethicone and a ceramide |
JP2007511512A (en) * | 2003-11-13 | 2007-05-10 | イーエルシー マネージメント エルエルシー | Transparent oil gelation system |
US7317068B2 (en) * | 2004-06-28 | 2008-01-08 | Inolex Investment Corporation | Complex polyol polyester polymer compositions for use in personal care products and related methods |
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2005
- 2005-07-11 EP EP05770892A patent/EP1768642A4/en not_active Withdrawn
- 2005-07-11 JP JP2007521524A patent/JP2008505968A/en active Pending
- 2005-07-11 US US11/178,824 patent/US20060019848A1/en not_active Abandoned
- 2005-07-11 KR KR1020077003302A patent/KR100876264B1/en active IP Right Grant
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- 2005-07-11 WO PCT/US2005/024416 patent/WO2006017203A1/en active Application Filing
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2010
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2011
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CA2573802A1 (en) | 2006-02-16 |
EP1768642A4 (en) | 2007-12-19 |
US20060019848A1 (en) | 2006-01-26 |
KR100876264B1 (en) | 2008-12-26 |
AU2005271921B2 (en) | 2008-11-27 |
EP1768642A1 (en) | 2007-04-04 |
KR20070035073A (en) | 2007-03-29 |
WO2006017203A1 (en) | 2006-02-16 |
US20110147999A1 (en) | 2011-06-23 |
JP2008505968A (en) | 2008-02-28 |
AU2005271921A1 (en) | 2006-02-16 |
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